期刊文献+
共找到5篇文章
< 1 >
每页显示 20 50 100
Incretin manipulation in diabetes management 被引量:6
1
作者 Joseph M Pappachan AV Raveendran Rajagopalan Sriraman 《World Journal of Diabetes》 SCIE CAS 2015年第6期774-781,共8页
Incretin-based therapies have revolutionized the medical management of type 2 diabetes mellitus(T2DM) in the 21 st century. Glucagon-like peptide-1(GLP-1) suppresses appetite and gastric motility, and has trophic effe... Incretin-based therapies have revolutionized the medical management of type 2 diabetes mellitus(T2DM) in the 21 st century. Glucagon-like peptide-1(GLP-1) suppresses appetite and gastric motility, and has trophic effects on pancreas, cardio-protective and renal effects. GLP-1 analogues and dipeptidyl peptidase-4 inhibitors form the incretin-based therapies. Significant reduction of hemoglobin A1 c when used as monotherapy and in combination regimens, favorable effects on body weight, and low risk of hypoglycemia are their unique therapeutic benefits. Their safety and tolerability are comparable to other anti-diabetic medications. Concern about elevated risk of pancreatitis has been discarded by two recent meta-analyses. This article discusses the therapeutic manipulation of incretin system for the management of T2 DM. 展开更多
关键词 incretin HORMONES incretin-based therapies Glucagon-like peptide-1 analogueS Dipeptidyl peptidase-4inhibitors PANCREATITIS
下载PDF
糖尿病药物治疗新进展——来自2005年欧洲糖尿病年会的最新信息 被引量:9
2
作者 王祥香 孙子林 《中国药科大学学报》 CAS CSCD 北大核心 2006年第2期105-110,共6页
结合2005年欧洲糖尿病年会的最新信息,对近年来已上市和正在试验及研发阶段的新型降糖药物,如非噻唑烷二酮类胰岛素增敏剂、肠促胰岛素、DPP-Ⅳ抑制剂、新型胰岛素类似物等进行综述。
关键词 噻唑烷二酮 肠促胰岛素 DPIP-Ⅳ抑制剂 胰岛素类似物 吸入胰岛素 口服胰岛素
下载PDF
人GLP-1类似物治疗2型糖尿病的研究进展 被引量:18
3
作者 蒋筠 彭永德 《世界临床药物》 CAS 2010年第2期74-77,97,共5页
人胰高血糖素样肽1(GLP-1)类似物已成为新一代降糖药。无论是上市的艾塞那肽和利拉鲁肽,还是处于临床研究阶段的taspoglutide,均在2型糖尿病临床研究中取得显著成果,如有效降糖、减轻体重和减少低血糖发生等。同时,人GLP-1类似物潜在的... 人胰高血糖素样肽1(GLP-1)类似物已成为新一代降糖药。无论是上市的艾塞那肽和利拉鲁肽,还是处于临床研究阶段的taspoglutide,均在2型糖尿病临床研究中取得显著成果,如有效降糖、减轻体重和减少低血糖发生等。同时,人GLP-1类似物潜在的益处与风险还有待进一步研究。 展开更多
关键词 2型糖尿病 肠促胰素 胰高血糖素样肽1 类似物
下载PDF
Role of incretins and glucagon receptor agonists in metabolic dysfunction-associated steatotic liver disease:Opportunities and challenges
4
作者 Chencheng Xie Naim Alkhouri Mohamed A Elfeki 《World Journal of Hepatology》 2024年第5期731-750,共20页
Metabolic dysfunction-associated steatotic liver disease(MASLD)has become the most common chronic liver disease worldwide,paralleling the rising pandemic of obesity and type 2 diabetes.Due to the growing global health... Metabolic dysfunction-associated steatotic liver disease(MASLD)has become the most common chronic liver disease worldwide,paralleling the rising pandemic of obesity and type 2 diabetes.Due to the growing global health burden and com-plex pathogenesis of MASLD,a multifaceted and innovative therapeutic approach is needed.Incretin receptor agonists,which were initially developed for diabetes management,have emerged as promising candidates for MASLD treatment.This review describes the pathophysiological mechanisms and action sites of three major classes of incretin/glucagon receptor agonists:glucagon-like peptide-1 receptor agonists,glucose-dependent insulinotropic polypeptide receptor agonists,and glucagon receptor agonists.Incretins and glucagon directly or indirectly impact various organs,including the liver,brain,pancreas,gastro-intestinal tract,and adipose tissue.Thus,these agents significantly improve glycemic control and weight management and mitigate MASLD pathogenesis.Importantly,this study provides a summary of clinical trials analyzing the effect-iveness and safety of incretin receptor agonists in MASLD management and provides an in-depth analysis highlighting their beneficial effects on improving liver function,hepatic steatosis,and intrahepatic inflammation.There are emerging challenges associated with the use of these medications in the real world,particularly adverse events,drug-drug interactions,and barriers to access,which are discussed in detail.Additionally,this review highlights the evolving role of incretin receptor agonists in MASLD management and suggests future research directions. 展开更多
关键词 Metabolic dysfunction-associated steatotic liver disease Metabolic dysfunction-associated steatohepatitis Glucagon-like peptide-1 glucose-dependent inulinotropic polypeptide Glucagon incretin Receptor agonist
下载PDF
葡萄糖依赖性肠促胰岛素类似物DAIa2GIP对大鼠膝关节损伤软骨的保护效应 被引量:2
5
作者 杨烜 韩鹏飞 +3 位作者 周新 卢建功 王世川 王宇泽 《中国组织工程研究》 CAS 北大核心 2019年第22期3549-3555,共7页
背景:已有研究证实,葡萄糖依赖性肠促胰岛素类似物DAla2GIP可直接调节成骨细胞的生长发育,但有关其在软骨细胞上的作用鲜有报道。目的:探讨葡萄糖依赖性肠促胰岛素类似物DAIa2GIP对SD大鼠骨性关节炎软骨损伤的保护效应及潜在机制。方法:... 背景:已有研究证实,葡萄糖依赖性肠促胰岛素类似物DAla2GIP可直接调节成骨细胞的生长发育,但有关其在软骨细胞上的作用鲜有报道。目的:探讨葡萄糖依赖性肠促胰岛素类似物DAIa2GIP对SD大鼠骨性关节炎软骨损伤的保护效应及潜在机制。方法:将50只雄性SD大鼠(山西医科大学实验动物中心提供)随机分5组,每组10只:正常对照组不进行任何干预;模型对照组、模型治疗组切断双后膝关节前交叉韧带、内侧副韧带并摘除内侧半月板;假手术对照组、假手术治疗组只打开双侧膝关节囊。造模后第8周,模型治疗组、假手术治疗组腹腔注射25 nmol/kg的DAIa2GIP,模型对照组、假手术对照组腹腔注射等量生理盐水,2次/周,注射8周。造模16周后,取各组大鼠膝关节,进行苏木精-伊红染色、番红O-固绿染色、透射电镜观察及免疫组织化学染色。实验方案经山西医科大学伦理委员会批准(2017008)。结果与结论:①苏木精-伊红染色显示,模型对照组软骨4层结构不清;模型治疗组软骨可见4层结构,软骨层较模型对照组增厚;其余3组软骨表面光滑,4层结构清晰;②番红O-固绿染色显示,模型对照组蛋白多糖表达明显不均匀,软骨厚度变薄;模型治疗组蛋白多糖表达基本均匀,软骨厚度较模型对照组增加;其余3组蛋白多糖表达均匀,软骨厚度适中;③透射电镜显示,模型对照组软骨细胞胞质内可见脂滴,线粒体、粗面内质网等细胞器消失;模型治疗组可见数量不等线粒体、粗面内质网等细胞器,并且结构基本恢复正常;其余组细胞结构正常;④免疫组织化学染色显示,与正常对照组比较,模型对照组胶原酶13蛋白表达升高(P<0.05),Ⅱ型胶原蛋白表达降低(P<0.05);与模型对照组比较,模型治疗组胶原酶13蛋白表达降低(P<0.05),Ⅱ型胶原蛋白表达升高(P<0.05);⑤结果表明,DAIa2GIP可能通过抑制关节软骨中胶原酶13表达、减少Ⅱ型胶原的破坏,对SD大鼠骨性关节炎中关节软骨发挥保护作用。 展开更多
关键词 葡萄糖依赖性肠促胰岛素类似物 GIP DAIa2GIP 骨性关节炎 胶原酶13 Ⅱ型胶原 软骨细胞 软骨损伤
下载PDF
上一页 1 下一页 到第
使用帮助 返回顶部